Sample information curated by ChIP-Atlas

Antigen

Antigen Class
TFs and others
Antigen
INTS3

Cell type

Cell type Class
Digestive tract
Cell type
DLD-1
Primary Tissue
Colon
Tissue Diagnosis
Adenocarcinoma

Attributes by original data submitter

Sample

source_name
DLD1
cell line
DLD1
cell type
colorectal adenocarcinoma cell line
chip antibody
INTS3
shRNA treatment
non target shRNA

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Lysates were clarified from sonicated cells and INTAC-DNA complexes were isolated with antibody. Libraries were prepared according to Vazyme's instructions accompanying the VAHTS Universal DNA Library Prep Kit (Vazyme ND607-02). Briefly, DNA was end-repaired using a combination of T4 DNA polymerase, E. coli DNA Pol I large fragment (Klenow polymerase) and T4 polynucleotide kinase. The blunt, phosphorylated ends were treated with Klenow fragment (32 to 52 exo minus) and dATP to yield a protruding 3- 'A' base for ligation of Illumina's adapters which have a single 'T' base overhang at the 3' end. After adapter ligation DNA was PCR amplified with Illumina primers for 15 cycles and library fragments of ~250 bp (insert plus adaptor and PCR primer sequences) were band isolated from an agarose gel. The purified DNA was captured on an Illumina flow cell for cluster generation. Libraries were sequenced on the Illumina HiSeq X Ten following the manufacturer's protocols.

Sequencing Platform

instrument_model
HiSeq X Ten

hg38

Number of total reads
60721478
Reads aligned (%)
82.0
Duplicates removed (%)
22.7
Number of peaks
7704 (qval < 1E-05)

hg19

Number of total reads
60721478
Reads aligned (%)
81.2
Duplicates removed (%)
22.9
Number of peaks
6957 (qval < 1E-05)

Base call quality data from DBCLS SRA